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神经元中 TRPCs 的生理功能与特性。

Physiological Function and Characterization of TRPCs in Neurons.

机构信息

Department of Basic Science, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND 58201, USA.

Calcium Signaling Laboratory, Research Service, Veterans Affairs Medical Center, Washington, DC 20422, USA.

出版信息

Cells. 2014 May 21;3(2):455-75. doi: 10.3390/cells3020455.

Abstract

Ca2+ entry is essential for regulating vital physiological functions in all neuronal cells. Although neurons are engaged in multiple modes of Ca2+ entry that regulates variety of neuronal functions, we will only discuss a subset of specialized Ca2+-permeable non-selective Transient Receptor Potential Canonical (TRPC) channels and summarize their physiological and pathological role in these excitable cells. Depletion of endoplasmic reticulum (ER) Ca2+ stores, due to G-protein coupled receptor activation, has been shown to activate TRPC channels in both excitable and non-excitable cells. While all seven members of TRPC channels are predominately expressed in neuronal cells, the ion channel properties, mode of activation, and their physiological responses are quite distinct. Moreover, many of these TRPC channels have also been suggested to be associated with neuronal development, proliferation and differentiation. In addition, TRPCs also regulate neurosecretion, long-term potentiation and synaptic plasticity. Similarly, perturbations in Ca2+ entry via the TRPC channels have been also suggested in a spectrum of neuropathological conditions. Hence, understanding the precise involvement of TRPCs in neuronal function and in neurodegenerative conditions would presumably unveil avenues for plausible therapeutic interventions for these devastating neuronal diseases.

摘要

钙离子内流对于调节所有神经元细胞的重要生理功能至关重要。尽管神经元参与了多种调节各种神经元功能的钙离子内流方式,但我们将仅讨论一组专门的、具有通透性的非选择性瞬时受体电位经典型(TRPC)通道,并总结它们在这些兴奋细胞中的生理和病理作用。由于 G 蛋白偶联受体的激活,内质网(ER)钙离子储存的耗竭已被证明可以在兴奋和非兴奋细胞中激活 TRPC 通道。虽然 TRPC 通道的所有七个成员主要在神经元细胞中表达,但离子通道特性、激活方式及其生理反应却大不相同。此外,许多这些 TRPC 通道也被认为与神经元的发育、增殖和分化有关。此外,TRPC 还调节神经分泌、长时程增强和突触可塑性。同样,通过 TRPC 通道的钙离子内流的扰动也被认为与一系列神经病理学状况有关。因此,了解 TRPC 在神经元功能和神经退行性疾病中的精确作用,可能会为这些破坏性神经元疾病的合理治疗干预提供途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f87/4092863/3f8da97c07df/cells-03-00455-g001.jpg

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